Bärbel Dittrich

Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

Karin Buiting, Shinji Saitoh, Bärbel Dittrich et al. · Nature Genetics · 1995 · 598 citations

Life Sciences, Genetics, Molecular Genetics +16

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

Bärbel Dittrich, Karin Buiting, Bernd Korn et al. · Nature Genetics · 1996 · 257 citations

Life Sciences, Genetics, Molecular Genetics +11

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

André Reis, Bärbel Dittrich, Valerie Greger et al. · PubMed · 1994 · 224 citations

Life Sciences, Genetics, Molecular Genetics +16

Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

Karin Buiting, Bärbel Dittrich, Stephanie Groß et al. · The American Journal of Human Genetics · 1998 · 216 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method

Michael Zeschnigk, Birgit Schmitz, Bärbel Dittrich et al. · Human Molecular Genetics · 1997 · 140 citations

Life Sciences, Genetics, Molecular Genetics +17